Hirschsprung disease, susceptibility to, 3
MONDO:0013383Mondo
Findings
No curated finding names Hirschsprung disease, susceptibility to, 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
3 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Aganglionic megacolonHPOHP:0002251
- 1 of 1 reported patient
- Long-segment aganglionic megacolonHPOHP:0011285
- 1 of 2 reported patients
- Total colonic aganglionosisHPOHP:0011286
- 1 of 2 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- GDNFHGNC:4232
- Limited · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
3 names
Resolves to: Hirschsprung disease, susceptibility to, 3
- Also called
- GDNF Hirschsprung diseaseHirschsprung disease caused by mutation in GDNFHirschsprung disease, susceptibility to, type 3